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	521.	Full monosomy 21: a clinically recognizable syndrome? [electronic resource] by Fryns, J P D'Hondt, F Goddeeris, P van den Berghe, H Producer: 19770922 In: Human genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	522.	Brief clinical report: the Dubowitz syndrome in a teenager. [electronic resource] by Fryns, J P Fabry, G Willemyns, F Van Den Berghe, H Producer: 19800523 In: American journal of medical genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	523.	Interstitial deletion of the distal long arm of chromosome 4. [electronic resource] by Sarda, P Lefort, G Fryns, J P Humeau, C Rieu, D Producer: 19920618 In: Journal of medical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	524.	The echographic diagnosis of fetal akinesia. A challenge towards etiological diagnosis and management. [electronic resource] by Grubben, C Gyselaers, W Moerman, P Vandenberghe, K Fryns, J P Producer: 19901220 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	525.	Angelman's syndrome and 15q11-q13 deletion. [electronic resource] by Fryns, J P Kleczowska, A Decock, P van den Berghe, H Producer: 19901220 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	526.	Ring chromosome 15: follow-up data on physical and psychological development. [electronic resource] by Fryns, J P Borghgraef, M Kleczkowska, A Van Den Berghe, H Producer: 19910503 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	527.	Normal phenotype and slight mental retardation in de novo distal 8p deletion (8pter----8p23.1:). [electronic resource] by Fryns, J P Kleczkowska, A Vogels, A Van den Berghe, H Producer: 19891201 In: Annales de genetique vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	528.	Distal 11q deletion: a specific clinical entity. [electronic resource] by Fryns, J P Kleczkowska, A Smeets, E Van den Berghe, H Producer: 19880212 In: Helvetica paediatrica acta vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	529.	Unusual chromosome 9 polymorphism and reproductive failure. [electronic resource] by Fryns, J P Kleczkowska, A Londers, L van den Berghe, H Producer: 19850821 In: Annales de genetique vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	530.	Mental retardation, deafness, skeletal abnormalities, and coarse face with full lips: confirmation of the Fountain syndrome. [electronic resource] by Fryns, J P Dereymaeker, A Hoefnagels, M Van den Berghe, H Producer: 19870514 In: American journal of medical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	531.	Complex chromosomal rearrangement involving chromosomes 11, 13 and 21. [electronic resource] by Kleczkowska, A Fryns, J P Jaeken, J Van den Berghe, H Producer: 19880829 In: Annales de genetique vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	532.	A newborn with the cat-eye syndrome. [electronic resource] by Fryns, J P Eggermont, E Veresen, H Van den Berghe, H Producer: 19730103 In: Humangenetik vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	533.	X-chromosome polysomy in the female: personal experience and review of the literature. [electronic resource] by Fryns, J P Kleczkowska, A Petit, P van den Berghe, H Producer: 19830715 In: Clinical genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	534.	Isodicentric (X)(q13): a new characteristic chromosomal anomaly in myeloproliferative syndrome? [electronic resource] by Petit, P Fryns, J P Masure, R Van Den Berghe, H Producer: 19830505 In: Cancer genetics and cytogenetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	535.	X-chromosomes attached by their long arm: case report and replication kinetics of the rearranged X-chromosome. [electronic resource] by Petit, P Fryns, J P Koumans, J van den Berghe, H Producer: 19821221 In: Clinical genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	536.	The Greig polysyndactyly craniofacial dysmorphism syndrome. [electronic resource] by Fryns, J P Coeck, W Mariën, P Van den Berghe, H Producer: 19810528 In: Acta paediatrica Belgica vol. Suppl 15 Availability: No items available. Save to lists Add to cart (remove)
	537.	Balanced transmission of centromeric fission products in man. [electronic resource] by Fryns, J P Bulcke, J Hens, L Van den Berghe, H Producer: 19800923 In: Human genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	538.	Apparently new autosomal dominant Spondyloepimetaphyseal dysplasia: gonadal mosaicism onset. [electronic resource] by de Ravel, T J L De Smet, L Fryns, J-P Producer: 20030312 In: Clinical dysmorphology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	539.	Asymmetrical Larsen syndrome in a young girl: a second example of somatic mosaicism in this syndrome. [electronic resource] by Debeer, Ph De Borre, L De Smet, L Fryns, J P Producer: 20030827 In: Genetic counseling (Geneva, Switzerland) vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	540.	Renal and urological tract malformations caused by a 22q11 deletion. [electronic resource] by Devriendt, K Swillen, A Fryns, J P Proesmans, W Gewillig, M Producer: 19960925 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.